Qualification & Experience   Qualifications for Full-Time Consultants: . MD/MS with a minimum of 5 years of experience.Retiring HODs and Senior Registrars looking for full time roles are also encouraged to apply.Qualifications for Senior Registrars: . MD/MS with a minimum of 2 years of experience.

ResponsibilitiesObserve structured online therapy sessions. Assist in case documentation and treatment planning. Support therapists working with Anxiety and Depression cases. Learn therapeutic approaches for OCD, Panic Attacks and Trauma/PTSD. Understand ADHD and Bipolar case frameworks. Assist in Relationship, Family and Marriage counselling cases. Gain exposure to Workplace Issues and EAP clients. Learn documentation standards and ethical compliance. Participate in supervision and case discussions. Develop understanding of CBT, REBT and other evidence-based models.Qualification & Experience   Be pursuing or have completed BA/MA/MSc in Psychology or related field. Have strong interest in clinical or counselling psychology. Be available for structured remote training sessions. Possess strong communication and documentation skills. Be committed to ethical and confidential practice. Have stable internet connection and work-from-home setup.

ResponsibilitiesConduct online psychiatric evaluations and follow-ups. Diagnose Anxiety, Depression and Mood Disorders. Manage ADHD and Bipolar Disorder cases. Treat OCD and Panic Disorders. Provide medication management for Trauma and PTSD. Address Addiction and Substance Abuse cases. Manage Insomnia and Sleep-related disorders. Provide Child & Teen psychiatric consultations when applicable. Collaborate with therapists for integrated care plans. Maintain detailed and confidential digital medical records. Follow ethical, legal and telemedicine prescription guidelines.Qualification & Experience   MBBS with MD/DNB in Psychiatry (Mandatory). Valid Medical Council registration in India. Minimum 2 years of clinical psychiatric experience preferred. Experience in medication management and psychiatric diagnosis. Ability to conduct structured video consultations. Commitment to ethical and evidence-based psychiatric practice. Reliable internet connection and private WFH setup.

ResponsibilitiesConduct structured online therapy sessions via secure video platform. Provide therapy for Anxiety, Depression and Stress Management. Treat OCD, Panic Attacks and Trauma/PTSD. Support clients with ADHD and Bipolar Disorder. Offer Relationship, Marriage and Couple Therapy. Provide Family and Child/Teen counselling. Address Workplace Issues and EAP clients. Deliver LGBTQ+ affirmative therapy when applicable. Provide Anger Management and Addiction counselling. Maintain accurate and confidential digital session notes. Develop personalised treatment plans. Monitor client progress and adjust therapeutic strategies. Follow ethical guidelines and professional standards of practice. Qualification & Experience   To qualify for this Therapist / Psychologist Job in India, you should have: Master’s degree in Psychology, Counselling, Clinical Psychology or related field. Valid RCI license (for Clinical Psychologists) where applicable. Minimum 2 years of therapy experience preferred. Experience in CBT/REBT/ERP or other structured modalities. Ability to conduct therapy effectively in an online setting. Strong communication and documentation skills. Commitment to ethical, confidential and evidence-based care. Stable internet connection and private work-from-home setup.

ResponsibilitiesExamine patients, diagnose illnesses, and prescribe appropriate treatment. Manage OPD and IPD patients efficiently with proper documentation. Handle emergency cases and provide immediate medical care.Qualification & Experience   Examine patients, diagnose illnesses, and prescribe appropriate treatment. Manage OPD and IPD patients efficiently with proper documentation. Handle emergency cases and provide immediate medical care. Monitor patient progress and update treatment plans accordingly. Coordinate with specialists, nurses, and other staff for patient care. Maintain accurate medical records and ensure compliance with hospital protocols. Educate patients and families about health conditions and preventive care.

ResponsibilitiesProvide direct patient care and monitor patient conditions regularly Assist doctors during examinations, treatments, and procedures Manage ICU/CCU/NICU patients with critical care support (as applicable) Maintain accurate patient records and nursing documentation Administer medications and injections as prescribed Ensure proper hygiene, infection control, and safety protocols Support OT procedures and maintain sterile environments (for OT Nurses) Supervise nursing staff and coordinate duties (for Nursing Supervisors) Educate patients and families about care and recovery Qualification & Experience   Strong clinical and patient care skills Knowledge of ICU/critical care practices (for ICU/CCU/NICU roles) Good communication and interpersonal skills Ability to handle emergency and high-pressure situations Knowledge of infection control and safety standards Teamwork and coordination abilities Attention to detail and record-keeping accuracy Compassionate and patient-centered approach Qualification & Salary Qualification: B.Sc. Nursing / GNM Salary may vary based on experience, skills, and clinical expertise.

Qualification & Experience                          Experience : MIN 1 YEAR TEACHING&2 YEARS CLINICAL EXPERIENCE                    Place : CALICUT Description : BSC NURSING       

ResponsibilitiesPrepare and review essential documentation, including GMP, GLP, and GCP manuals. Responsible and Managing of Document Management Life Cycle and Record Management Issuance, Retrieval, Archival and Control of GMP Documents/Records and DSMs (GMP documents) through Manual and Electronic systems. Secure bin management Knowledge on PDOCs, p-log and SDS Applications Ensure compliance with Enterprise Records Retention Schedule (ERRS) maintained by the enterprise records and Information Management (eRIM) group. Location mapping & tracking of documents/ records archived in Active Record Centers. Competency in MS office, Adobe Acrobat and documentation data base systems Execute tasks supporting Quality Systems functions and oversee Documentation Control and administrative functions of the DMS repository. Qualification & ExperienceBachelor's Degree (Chemistry/Pharmacy) with 4+ Years of Experience or Master's Degree (Chemistry/Pharmacy) with 3+ Years of Experience Proficiency in Document Management and Control Experience with Computer Software Validation Concepts Familiarity with regulatory requirements and compliance standards Effective communication skills

ResponsibilitiesSupport general compliance activities in line with departmental needs (e.g., act as SOP manager, training responsible person, 1QEM key user; support KQI reporting and quality monitoring, and QMS implementation). Support third party management–related processes, including administrative and system support (e.g. site ID creation, system verifications, dashboards, data management, due?date tracking and communications). Support third party oversight related activities, including audit administration review of third-party GMP documentation and BD&L deals. Author and review GxP documentation. Support the filing and archiving of GxP records in accordance with applicable procedures. Contribute to continuous improvement of compliance and third-party management processes. Support project-related activities (e.g., developing new tools and implementing new processes).

Responsibilities Lead compilation and submission of regulatory dossiers for new drugs, line extensions, additional indications, and lifecycle changes (renewals, site registrations, production transfers). Manage Clinical Trial Application (CTA) submissions and ensure compliance throughout study lifecycle. Support development and execution of regulatory strategies for pipeline products to enable timely market access. Ensure timely execution of post-approval regulatory commitments including PSURs, CMC variations, and labeling updates. Drive regulatory compliance tracking, including monitoring submissions, approvals, and ongoing obligations with Health Authorities. Collaborate with cross-functional stakeholders (Legal, QA, Supply Chain, Global teams) to ensure seamless regulatory execution and supply continuity. Support critical regulatory changes (e.g., site changes, legal entity updates, supply chain changes) with minimal disruption to business. Contribute to regulatory intelligence gathering and provide guidance on evolving regulatory requirements. Ensure data integrity and compliance through maintenance of regulatory databases and audit readiness. Drive process improvements, CAPA management, and compliance oversight to enhance regulatory efficiency and inspection readiness. Qualification & ExperienceBachelor’s degree in Pharmacy / Life Sciences / Health Sciences/ Chemistry. 5 + years of hands-on experience in Regulatory Affairs within Indian regulatory framework, preferably in a multinational pharmaceutical environment. Strong experience in dossier compilation and HA submissions (NDAs, CTAs, lifecycle management). Good understanding of Indian regulatory requirements (e.g., CDSCO processes, clinical trial regulations, post-approval compliance). Strong cross-functional collaboration and stakeholder management skills. Effective communication (written and verbal) and interpersonal skills. Desirable Requirements Post-graduate degree in Pharmacy / Life Sciences / Regulatory Affairs/ Chemistry.